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    • 11. 发明授权
    • Continuous preparation of acetic acid esters
    • 连续制备乙酸酯
    • US4370491A
    • 1983-01-25
    • US263470
    • 1981-05-14
    • Kaspar BottGerd KaibelHerwig HoffmannRudolf IrnichEberhard Schaefer
    • Kaspar BottGerd KaibelHerwig HoffmannRudolf IrnichEberhard Schaefer
    • C07C67/03B01D3/36C07C67/02C07C69/14C07C67/06
    • C07C67/03Y10S203/06
    • A process for the preparation of acetic acid esters CH.sub.3 --CO--O--R.sup.1 (I, R.sup.1 =an organic radical other than methyl and ethyl) by alkali-catalyzed trans-esterification of an acetic acid ester CH.sub.3 --CO--O--R.sup.2 (II, R.sup.2 =methyl or ethyl) with an alcohol R.sup.1 --OH (III), accompanied by elimination of the alcohol R.sup.2 --OH (IV), wherein(a) the trans-esterification reaction is carried out in the middle section K.sub.M of a distillation column K, the alcohol III being fed as liquid into the upper zone and the ester II into the lower zone of K.sub.M,(b) the alkaline catalyst is introduced into the upper part K.sub.U of K,(c) the alcohol IV, or a mixture of IV and the ester II, is taken off the top of the column,(d) the mixture obtained from (c) (unless the alcohol IV alone is obtained) is separated in the column section K.sub.U or in a stripper column K.sub.S into IV and the azeotrope of II and IV, and the latter is recycled to the lower zone of K.sub.M,(e) the ester I is taken as vapor or liquid from the lower zone of the lower section K.sub.L of K and(f) the catalyst is either removed, or recycled to K.sub.U, in a conventional manner.
    • 通过乙酸酯CH3-CO-O-R2的碱催化反式酯化制备乙酸酯CH 3 -CO-O-R 1(I,R 1 =甲基和乙基以外的有机基)的方法 II,R 2 =甲基或乙基)与醇R 1 -OH(III)反应,同时除去醇R 2 -OH(Ⅳ),其中(a)酯交换反应在 蒸馏塔K,醇III作为液体进料到上部区域,酯II进入KM的下部区域,(b)将碱性催化剂引入K的上部KU,(c)醇IV,或 将IV和酯II的混合物从柱顶部取出,(d)从(c)获得的混合物(除非单独获得醇IV)在柱部分KU或汽提塔KS中分离 进入IV和II和IV的共沸物,后者再循环到KM的下部区域,(e)将酯I作为蒸汽或液体从下部KL的下部区域中取出 的K和(f)催化剂以常规方式被去除或再循环至KU。
    • 13. 发明授权
    • Ethylenically unsaturated compounds
    • 乙烯不饱和化合物
    • US5202483A
    • 1993-04-13
    • US663302
    • 1991-03-01
    • Gerd RehmerKaspar Bott
    • Gerd RehmerKaspar Bott
    • C07C49/76C07C59/125C07C69/736C07C233/31C07C255/13C08F20/58C09J7/02C09J133/06C09J133/24
    • C07C233/31C08F20/58C09J133/24C09J7/021C07C2102/10
    • Ethylenically unsaturated compounds of the general formula I ##STR1## where R.sub.1 is alkyl of 1 to 4 carbon atoms, cyclopropyl, cyclopentyl, cyclohexyl, phenyl or phenyl in which some or all of the hydrogen atoms have been replaced by radicals R.sup.4, not more than two substituents R.sup.4 being identical, or R.sup.1 together with R.sup.2 or together with R.sup.6 forms a --CH.sub.2 --CH.sub.2 -- or --CH.sub.2 --CH.sub.2 --CH.sub.2 -- bridge,R.sup.4 is alkyl of 1 to 24 carbon atoms, --OH, --O--R.sup.7, --S--R.sup.7, ##STR2## R.sup.2 or R.sup.6, independently of one another, both are hydrogen, or one of the radicals R.sup.4, or, where R.sup.1 is aryl,R.sup.2 or R.sup.6 is a direct bond to R.sup.1 in the ortho-position with respect to the carbonyl group, andR.sup.3 and R.sup.5 are each hydrogen, one of the radicals R.sup.4 or a group the general formula II ##STR3## where R.sup.7 and R.sup.8 are each alkyl of 1 to 4 carbon atoms,R.sup.9 is cycloalkyl of 5 or 6 carbon atoms,R.sup.10 is hydrogen or alkyl of 1 to 4 carbon atoms andR.sup.11 is hydrogen or alkyl of 1 to 4 carbon atoms,with the proviso that either R.sup.3 or R.sup.5 is a group of the general formula II,are suitable for the preparation of polymers which, after exposure to actinic radiation, have increased internal strength.
    • 其中R 1为1至4个碳原子的烷基,环丙基,环戊基,环己基,苯基或苯基的通式I(I)的烯键式不饱和化合物,其中部分或全部氢原子已被基团R 4取代, 不多于两个取代基R 4相同,或者R 1与R 2或与R 6一起形成-CH 2 -CH 2 - 或-CH 2 -CH 2 -CH 2 - 桥,R 4是1至24个碳原子的烷基,-OH,-O -R7,-S-R7, R2或R6彼此独立,均为氢或基团R4之一,或其中R1为芳基,R2或R6 是相对于羰基在邻位的R 1的直接键合,R 3和R 5各自是氢,基团R 4或通式II(II)中的一个基团,其中R 7和R 8各自为 1至4个碳原子的烷基,R 9为5或6个碳原子的环烷基,R 10为氢或1至4个碳原子的烷基,R 11为氢或1至4个碳原子的烷基,条件是任一 R3或R5是通式II的基团,适用于制备聚合物,其在曝光于光化辐射之后具有增加的内部强度。
    • 15. 发明授权
    • Preparation of carbonyl halides
    • 制备羰基卤化物
    • US5041649A
    • 1991-08-20
    • US68013
    • 1987-06-29
    • Kaspar Bott
    • Kaspar Bott
    • B01J27/125B01J27/00C07B61/00C07C51/00C07C51/58C07C53/38C07C57/64C07C61/13C07C67/00
    • C07C51/58
    • Carbonyl halides I ##STR1## where R.sup.1 is H, alkyl, cycloalkyl, haloalkyl or halocycloalkyl,R.sup.2 and R.sup.3 are each alkyl, cycloalkyl, haloalkyl or halocycloalkyl and may furthermore be bonded to one another to form a 5-membered to 7-membered ring andis halogen,are prepared by reacting an alkyl halide II ##STR2## with carbon monoxide under superatmospheric pressure in the presence of a catalytic amount ofa) aluminum bromide and in the presence or absence of a solvent orb) aluminum chloride or bromide and in the presence of a halohydrocarbon and a carbonyl halide of the formula IIIR.sup.4 --CH.sub.2 --CO--Hal (III) where R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl and Hal is halogen.
    • 羰基卤化物I,其中R 1是H,烷基,环烷基,卤代烷基或卤代环烷基,R 2和R 3各自是烷基,环烷基,卤代烷基或卤代环烷基,并且还可以彼此键合形成5元至7元 环和卤素通过烷基卤化物II II与一氧化碳在超大气压下在催化量的溴化铝存在下和在存在或不存在溶剂的情况下反应制备,或b)氯化铝或 在卤代烃和式III的卤化碳R4-CH2-CO-Hal(Ⅲ)的存在下,其中R4是氢或C1-C4-烷基,Hal是卤素。
    • 16. 发明授权
    • Preparation of carboxylic esters
    • 羧酸酯的制备
    • US4889950A
    • 1989-12-26
    • US235610
    • 1988-08-24
    • Kaspar BottHorst HartmannJosef Guth
    • Kaspar BottHorst HartmannJosef Guth
    • C07C67/08C07C69/54
    • C07C67/08C07C67/54
    • Carboxylic esters are prepared by reacting carboxylic acids with low-boiling alcohols by charging the reaction mixture to a 1st distillation column, withdrawing the reaction components carboxylic ester, water and unconverted alcohol as overhead product and charging this overhead product to a 2nd distillation column, from which(a) the overhead product comprises the alcohol or an azeotropic mixture of alcohol and water or alcohol and esteer, this overhead product being recycled into the esterification reaction(b) a liquid side product comprising carboxylic ester and water is withdrawn from the stripping section and separated in a phase separating vessel into water and carboxylic ester and the carboxylic ester is returned into the distillation column below the side takeoff point, and(c) the bottom product removed is the carboxylic ester.
    • 通过将反应混合物装入第一蒸馏塔,将反应组分羧酸酯,水和未转化的醇作为塔顶产物取出并将该塔顶产物装入第二蒸馏塔,由羧酸与低沸点醇反应制备羧酸酯,由 其中(a)塔顶产物包含醇或醇或水或醇的共沸混合物和催化剂,该塔顶产物被再循环到酯化反应中(b)包含羧酸酯和水的液体副产物从汽提段 并在相分离容器中分离成水和羧酸酯,并且羧酸酯在侧馏出点下方返回到蒸馏塔中,(c)除去的底部产物是羧酸酯。